PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
25642214-0	2014	Activity of the response regulator CiaR in mutants of Streptococcus pneumoniae R6 altered in acetyl phosphate production.	acetyl phosphate	93-109	ciaR	Streptococcus pneumoniae R6	35-39
26300871-6	2015	The negative effect exerted by the absence of CpxA on the expression of SPI-1 genes was counteracted by the absence of CpxR or by the absence of the two enzymes, AckA and Pta, which render acetyl-phosphate that phosphorylates CpxR.	acetyl phosphate	189-205	Spi-1 proto-oncogene	Homo sapiens	72-77
11179649-0	2001	Involvement of acetyl phosphate in the in vivo activation of the response regulator ComA in Bacillus subtilis.	acetyl phosphate	15-31	COMA	Homo sapiens	84-88
22903977-1	2012	Acetate kinase (ACK) catalyzes the reversible synthesis of acetyl phosphate by transfer of the gamma-phosphate of ATP to acetate.	acetyl phosphate	59-75	tyrosine kinase non receptor 2	Homo sapiens	16-19
22903977-7	2012	Characterizations of enzyme variants altered in the putative acetate/acetyl phosphate binding pocket suggested that acetyl phosphate binding is not mediated solely through a hydrophobic interaction but also through the phosphoryl group, as for the M. thermophila ACK.	acetyl phosphate	69-85	tyrosine kinase non receptor 2	Homo sapiens	263-266
22903977-7	2012	Characterizations of enzyme variants altered in the putative acetate/acetyl phosphate binding pocket suggested that acetyl phosphate binding is not mediated solely through a hydrophobic interaction but also through the phosphoryl group, as for the M. thermophila ACK.	acetyl phosphate	116-132	tyrosine kinase non receptor 2	Homo sapiens	263-266
19851741-0	2009	Evidence against the physiological role of acetyl phosphate in the phosphorylation of the ArcA response regulator in Escherichia coli.	acetyl phosphate	43-59	arginine deiminase	Escherichia coli	90-94
19851741-3	2009	ArcA has been shown to be able to autophosphorylate in vitro at the expense of acetyl-P.	acetyl phosphate	79-87	arginine deiminase	Escherichia coli	0-4
19851741-5	2009	Our results indicate that acetyl phosphate can modulate the expression of ArcA-P target genes only in the absence of ArcB.	acetyl phosphate	26-42	arginine deiminase	Escherichia coli	74-78
19851741-6	2009	Therefore, the acetyl phosphate dependent ArcA phosphorylation route does not seem to play a significant role under physiological conditions.	acetyl phosphate	15-31	arginine deiminase	Escherichia coli	42-46
18430561-3	2008	POX catalyzes the degradation of pyruvate to acetylphosphate, CO(2) and H(2)O(2) in the presence of phosphate and oxygen.	acetyl phosphate	45-60	proline dehydrogenase 1	Homo sapiens	0-3
16630631-8	2006	Also similarly to the case of Acs-mediated acetylation, the phosphodonors of CheY, CheA and acetyl phosphate, each inhibited the autoacetylation of CheY, whereas the phosphatase of CheY, CheZ, enhanced it.	acetyl phosphate	92-108	acyl-CoA synthetase short chain family member 2	Homo sapiens	30-33
16444581-5	2006	The compounds acetyl phosphate, carbamoyl phosphate, dihydroxyacetone phosphate and imidodiphosphate were found to stimulate AK activity in a dose-dependent manner comparable to that seen with Pi.	acetyl phosphate	14-30	adenosine kinase	Homo sapiens	125-127
25267444-4	2014	While transketolase catalyzes the reversible transfer of 2-carbon ketol fragments in a reaction analogous to that of transaldolase, phosphoketolase forms acetyl phosphate as final product in a reaction that comprises ketol cleavage, dehydration and phosphorolysis.	acetyl phosphate	154-170	transaldolase 1	Homo sapiens	117-130
21173314-8	2011	A recent study reported that the overexpression of BB0589, a phosphate acetyl-transferase (Pta) that converts acetyl-phosphate to acetyl-coenzyme A (CoA), led to the inhibition of RpoS and OspC expression, suggesting that acetyl-phosphate is an activator of Rrp2.	acetyl phosphate	110-126	OspC	Borreliella burgdorferi	189-193
20862323-0	2010	Role of acetyl-phosphate in activation of the Rrp2-RpoN-RpoS pathway in Borrelia burgdorferi.	acetyl phosphate	8-24	rhomboid like 2	Homo sapiens	46-50
16276532-4	2006	About 82% yield of dTDP-L-rhamnose was obtained based on initial dTMP concentration at 20 mM dTMP, 1 mM ATP, 10 mM NADH, 60 mM acetyl phosphate, and 80 mM glucose-1-phosphate.	acetyl phosphate	127-143	TAR DNA-binding protein-43 homolog	Drosophila melanogaster	19-23
11179649-3	2001	In this study we suggested that the ComA could also be activated by a small molecule phospho-donor, acetyl phosphate.	acetyl phosphate	100-116	COMA	Homo sapiens	36-40
11179649-6	2001	As Pta is responsible for the catalysis for conversion of acetyl coenzyme A to acetyl phosphate, we conclude that the expression of srfA seen in the comP mutant is mainly due to the activation of ComA by acetyl phosphate.	acetyl phosphate	79-95	COMA	Homo sapiens	196-200
11179649-6	2001	As Pta is responsible for the catalysis for conversion of acetyl coenzyme A to acetyl phosphate, we conclude that the expression of srfA seen in the comP mutant is mainly due to the activation of ComA by acetyl phosphate.	acetyl phosphate	204-220	COMA	Homo sapiens	196-200
10830874-1	2000	Studies on acetyl phosphate (AcP2-), one of the so-called "energy-rich" mixed-acid anhydrides, are summarized.	acetyl phosphate	11-27	acid phosphatase 2, lysosomal	Homo sapiens	29-33
11671407-5	1997	The effects of inhibition of hexokinase by phosphoenolpyruvate and acetyl phosphate on cofactor regeneration are discussed.	acetyl phosphate	67-83	hexokinase	Saccharomyces cerevisiae S288C	29-39
9235924-0	1997	Independence of two conformations of sarcoplasmic reticulum Ca2+-ATPase molecules in hydrolyzing acetyl phosphate.	acetyl phosphate	97-113	dynein axonemal heavy chain 8	Homo sapiens	65-71
9882653-4	1999	A heterologous system consisting of acetyl phosphate, the bacterial chemotaxis response regulator CheY, and YPD1 has been developed as an efficient means of phosphorylating SLN1 and SSK1 in vitro.	acetyl phosphate	36-52	histidine kinase	Saccharomyces cerevisiae S288C	173-177
9882653-4	1999	A heterologous system consisting of acetyl phosphate, the bacterial chemotaxis response regulator CheY, and YPD1 has been developed as an efficient means of phosphorylating SLN1 and SSK1 in vitro.	acetyl phosphate	36-52	mitogen-activated protein kinase kinase kinase SSK1	Saccharomyces cerevisiae S288C	182-186
9334214-4	1997	2) Immediately upon cell lysis, the pH stability curves of metabolically labeled native [32P]prothymosin alpha or a [32P]histidine-tagged variant resembled the pH stability curve of acetyl phosphate.	acetyl phosphate	182-198	prothymosin alpha pseudogene 9	Homo sapiens	93-110
7559459-3	1995	In this report, we demonstrate that the cytoplasmic domain of VanS (including residues Met95 to Ser384) is capable of high level activation (> 500 fold) of the Escherichia coli response regulator PhoB in vivo in the absence of its signaling kinases PhoR, CreC (PhoM), or acetyl phosphate synthesis.	acetyl phosphate	274-290	VanS protein	Enterococcus faecium	62-66
8981985-9	1997	Activation of the VanR response regulator in the absence of VanS may involve autophosphorylation of VanR with acetyl phosphate or phosphorylation by a heterologous histidine protein kinase.	acetyl phosphate	110-126	VanR	Enterococcus faecium	18-22
8981985-9	1997	Activation of the VanR response regulator in the absence of VanS may involve autophosphorylation of VanR with acetyl phosphate or phosphorylation by a heterologous histidine protein kinase.	acetyl phosphate	110-126	VanS protein	Enterococcus faecium	60-64
8981985-9	1997	Activation of the VanR response regulator in the absence of VanS may involve autophosphorylation of VanR with acetyl phosphate or phosphorylation by a heterologous histidine protein kinase.	acetyl phosphate	110-126	VanR	Enterococcus faecium	100-104
7615538-7	1995	At this pH, calcium binding to the monomeric ATPase, solubilized with dodecyloctaethylenglycol monoether, was studied by examining 45Ca2+ binding to the ATPase and calcium dependence of its phosphorylation, fluorescence intensity, ATP-hydrolysis at a low (5 microM) concentration of ATP, and acetyl phosphate hydrolysis.	acetyl phosphate	292-308	dynein axonemal heavy chain 8	Homo sapiens	45-51
7643383-11	1995	Incubation with the phospho-donor, acetyl phosphate, allowed both MBP-NarP and MBP-NarL to protect the -44.5 region of the aeg-46.5 operon control region from DNase I cleavage.	acetyl phosphate	35-51	myelin basic protein	Homo sapiens	66-69
7643383-11	1995	Incubation with the phospho-donor, acetyl phosphate, allowed both MBP-NarP and MBP-NarL to protect the -44.5 region of the aeg-46.5 operon control region from DNase I cleavage.	acetyl phosphate	35-51	neuronal pentraxin 2	Homo sapiens	70-74
7643383-11	1995	Incubation with the phospho-donor, acetyl phosphate, allowed both MBP-NarP and MBP-NarL to protect the -44.5 region of the aeg-46.5 operon control region from DNase I cleavage.	acetyl phosphate	35-51	myelin basic protein	Homo sapiens	79-82
7532003-3	1995	To elucidate the molecular conformation and interactions in solution, a family of highly resolved nuclear magnetic resonance (NMR) structures was determined for the src SH2 domain complexed with a high-affinity phosphorylated pentapeptide, acetyl-p YEEIE-OH.	acetyl phosphate	240-248	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	165-168
1532553-2	1992	After reduction by sodium borohydride, oATP binds covalently to the catalytic adenosine-nucleotide-binding site of the enzyme, resulting in 85% loss of acetyl-phosphate-driven Ca2+ uptake and ATP-hydrolysing ability.	acetyl phosphate	152-168	solute carrier organic anion transporter family member 1A2	Homo sapiens	39-43
8393448-3	1993	Addition of acetyl phosphate to a Na(+)-bound enzyme (NaE1) to accumulate acetate-sensitive phosphoenzyme (E1P) induced a faster and greater FITC fluorescence decrease when excited at 470 nm than at 305 nm.	acetyl phosphate	12-28	NEDD8 activating enzyme E1 subunit 1	Sus scrofa	54-58
8161518-3	1994	Alternatively, about an 8% abundance of P-VanR was produced with acetyl phosphate.	acetyl phosphate	65-81	VanR	Enterococcus faecium	42-46
8161518-8	1994	A mutant VanR(D53A) was shown to be incompetent for phosphorylation by phosphorylated MBP-VanS or by acetyl phosphate; however, it still bound DNA specifically, albeit with low affinity.	acetyl phosphate	101-117	VanR	Enterococcus faecium	9-13
1939235-4	1991	The protein C component also catalyzes the arsenate-dependent decomposition of acetyl phosphate.	acetyl phosphate	79-95	protein C, inactivator of coagulation factors Va and VIIIa	Homo sapiens	4-13
1939235-5	1991	Reaction of protein C with iodoacetate inhibits its ability to decompose acetyl phosphate, but this inactivation of the enzyme by alkylation is prevented in the presence of the substrate indicating the formation of an unreactive enzyme-bound acetylthiol ester.	acetyl phosphate	73-89	protein C, inactivator of coagulation factors Va and VIIIa	Homo sapiens	12-21
34626299-3	2021	Acylphosphatase 1 is a cytosolic enzyme that produces acetic acid from acetyl phosphate and plays an important role in cancer progression.	acetyl phosphate	71-87	acylphosphatase 1	Homo sapiens	0-17
13246635-1	1955	Acetyl phosphate and 1,3-diphosphoglycerate react with glyceraldehyde-3-phosphate dehydrogenase to form relatively stable enzyme substrate compounds.	acetyl phosphate	0-16	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	55-95
3036067-0	1987	Interaction of acetyl phosphate and carbamyl phosphate with plant phosphoenolpyruvate carboxylase.	acetyl phosphate	15-31	phosphoenolpyruvate carboxykinase 1	Homo sapiens	66-97
2932440-3	1985	Covalent labeling of the Ca2+-ATPase by fluorescein 5"-isothiocyanate inhibited both the ATP and acetyl phosphate-dependent Ca2+ transport.	acetyl phosphate	97-113	dynein axonemal heavy chain 8	Homo sapiens	30-36
4507619-1	1972	The sulfenic acid form of glyceraldehyde-3-phosphate dehydrogenase (EC 1.2.1.12), which is an acyl phosphatase, will catalyze an acetyl phosphate-Pi exchange reaction.	acetyl phosphate	129-145	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	26-66
4250734-0	1970	[Effect of acetylphosphate and inorganic phosphate on the interaction of Na plus minus K plus minus ATPase with ouabain].	acetyl phosphate	11-26	dynein axonemal heavy chain 8	Homo sapiens	100-106
2835101-4	1988	At 20 degrees C, in the presence of 1 mM RbCl and no Mg2+, acetyl phosphate did not affect E2(Rb); with 3 mM MgCl2, acetyl phosphate stimulated a release of Rb from E2(Rb) both in the presence and absence of RbCl in the incubation mixture.	acetyl phosphate	116-132	cystatin 12, pseudogene	Homo sapiens	165-171
163256-5	1975	Incubation of the glyceraldehyde 3-phosphate dehydrogenase with glyceraldehyde 3-phosphate, acetyl phosphate, iodoacetic acid, or iodosobenzoate inhibits the formation of the acid-stable complex with 3-pyridinealdehyde-NAD.	acetyl phosphate	92-108	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	18-58
31948874-3	2020	now show that early metabolic alterations in macrophages driven by LPS signaling serve to increase the acetyl-CoA pool via citrate metabolism by the ATP-citrate lyase (ACLY), leading to histone acetylation and regulation of TLR-driven gene expression.	acetyl phosphate	103-109	ATP citrate lyase	Homo sapiens	149-166
31960561-4	2020	Quasi-in-situ solid state NMR detects C 2 species of acetyl [-COCH 3 ] bonding with an oxygen, ethyl [-CH 2 CH 3 ] bonding with a Zn site, and epoxyethane molecules adsorbing on a Zn site and a Bronsted acid site of the catalyst, respectively.	acetyl phosphate	53-59	cochlin	Homo sapiens	62-66
32015101-0	2020	Mutual balance of histone deacetylases HDAC1, HDAC2, and the acetyl reader ATAD2 regulates the level of acetylation of histone H4 on nascent chromatin of human cells.	acetyl phosphate	28-34	histone deacetylase 1	Homo sapiens	39-44
32015101-0	2020	Mutual balance of histone deacetylases HDAC1, HDAC2, and the acetyl reader ATAD2 regulates the level of acetylation of histone H4 on nascent chromatin of human cells.	acetyl phosphate	28-34	histone deacetylase 2	Homo sapiens	46-51
32015101-0	2020	Mutual balance of histone deacetylases HDAC1, HDAC2, and the acetyl reader ATAD2 regulates the level of acetylation of histone H4 on nascent chromatin of human cells.	acetyl phosphate	28-34	ATPase family AAA domain containing 2	Homo sapiens	75-80
31878768-4	2020	Transcriptional activity of RUNX2 is regulated at the post-translational level by various enzymes including kinases, acetyl transferases, deacetylases, ubiquitin E3 ligases, and prolyl isomerases.	acetyl phosphate	117-123	RUNX family transcription factor 2	Homo sapiens	28-33
13163071-0	1954	Acetyl phosphate formation catalyzed by glyceraldehyde-3-phosphate dehydrogenase.	acetyl phosphate	0-16	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	40-80
13163072-0	1954	Transfer reactions of acetyl phosphate catalyzed by glyceraldehyde-3-phosphate dehydrogenase.	acetyl phosphate	22-38	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	52-92
31792920-7	2020	Moreover, high glucose increased the protein levels of p53, acetyl-p53 and p21.	acetyl phosphate	60-66	tumor protein p53	Homo sapiens	67-70
32019286-11	2020	Tyrosine metabolism also generated nuclear acetyl-CoA to acetylate and stabilize Foxd3, thereby allowing CD13+ CSCs cells to sustain quiescence and resistance to chemotherapeutic agents.	acetyl phosphate	43-49	forkhead box D3	Homo sapiens	81-86
32019286-11	2020	Tyrosine metabolism also generated nuclear acetyl-CoA to acetylate and stabilize Foxd3, thereby allowing CD13+ CSCs cells to sustain quiescence and resistance to chemotherapeutic agents.	acetyl phosphate	43-49	alanyl aminopeptidase, membrane	Homo sapiens	105-109
31587155-1	2020	BACKGROUND: Ubiquitin-specific protease 22 (USP22) is described as a key subunit of the Spt-Ada-Gcn5 acetyl transferase complex, which plays an important role in the prognosis and resistance to chemotherapy drugs in hepatocellular carcinoma (HCC).	acetyl phosphate	101-107	ubiquitin specific peptidase 22	Homo sapiens	12-42
31587155-1	2020	BACKGROUND: Ubiquitin-specific protease 22 (USP22) is described as a key subunit of the Spt-Ada-Gcn5 acetyl transferase complex, which plays an important role in the prognosis and resistance to chemotherapy drugs in hepatocellular carcinoma (HCC).	acetyl phosphate	101-107	ubiquitin specific peptidase 22	Homo sapiens	44-49
31926163-4	2020	SIRT6, which is an ADP-ribosyltransferase and NAD+-dependent deacetylase of acetyl and long-chain fatty acyl groups, playing central roles in lipid and glucose metabolism, is closely related to the occurrence of diabetes and obesity caused by overnutrition and aging.	acetyl phosphate	63-69	sirtuin 6	Bos taurus	0-5
32069267-0	2020	TNFalpha regulates diabetic macrophage function through the histone acetyl-transferase, MOF.	acetyl phosphate	68-74	tumor necrosis factor	Mus musculus	0-8
32069267-0	2020	TNFalpha regulates diabetic macrophage function through the histone acetyl-transferase, MOF.	acetyl phosphate	68-74	K(lysine) acetyltransferase 8	Mus musculus	88-91
32069267-5	2020	Males absent on the first (MOF) is a histone acetyl-transferase (HAT) that has been shown be a co-activator of TNFalpha-signaling and promote NFkappaB-mediated gene transcription in prostate cancer cell lines.	acetyl phosphate	45-51	K(lysine) acetyltransferase 8	Mus musculus	27-30
32069267-5	2020	Males absent on the first (MOF) is a histone acetyl-transferase (HAT) that has been shown be a co-activator of TNFalpha-signaling and promote NFkappaB-mediated gene transcription in prostate cancer cell lines.	acetyl phosphate	45-51	tumor necrosis factor	Mus musculus	111-119
32069267-5	2020	Males absent on the first (MOF) is a histone acetyl-transferase (HAT) that has been shown be a co-activator of TNFalpha-signaling and promote NFkappaB-mediated gene transcription in prostate cancer cell lines.	acetyl phosphate	45-51	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	142-150
31709711-9	2020	ATF3 represses the association of the activating mark, acetyl histone H4 lysine 8 (H4AcK8) at the promoter of Ch25h.	acetyl phosphate	55-61	activating transcription factor 3	Mus musculus	0-4
31815277-9	2020	Chromatin immunoprecipitation assays using acetyl-H3K56 or acetyl-H3K122 antibody revealed that aspirin blocked the TGFbeta2-induced acetylation of H3K56 and H3K122 at the promoter regions of ACTA2 and COL1A.	acetyl phosphate	43-49	transforming growth factor beta 2	Homo sapiens	116-124
31815277-9	2020	Chromatin immunoprecipitation assays using acetyl-H3K56 or acetyl-H3K122 antibody revealed that aspirin blocked the TGFbeta2-induced acetylation of H3K56 and H3K122 at the promoter regions of ACTA2 and COL1A.	acetyl phosphate	59-65	transforming growth factor beta 2	Homo sapiens	116-124
31948874-3	2020	now show that early metabolic alterations in macrophages driven by LPS signaling serve to increase the acetyl-CoA pool via citrate metabolism by the ATP-citrate lyase (ACLY), leading to histone acetylation and regulation of TLR-driven gene expression.	acetyl phosphate	103-109	ATP citrate lyase	Homo sapiens	168-172
31667988-3	2020	Incubations using pS9 led to the formation of an acetyl conjugation in case of 2-AI and merely a hydroxylamine for NM-2-AI.	acetyl phosphate	49-55	taste 2 receptor member 2, pseudogene	Homo sapiens	18-21
31814524-8	2020	Furthermore, CHIP assay confirmed that acetyl-H3 directly combined with the promoter region of IL-8 to promote its transcription.	acetyl phosphate	39-45	C-X-C motif chemokine ligand 8	Homo sapiens	95-99
31814524-9	2020	Therefore, the results of this study demonstrated that 4-PBA-mediated inhibition of HDAC activity could induce EMT in gastric cancer cells via acetyl-histone-mediated IL-8 upregulation, and the downstream Gab2/ERK activation.	acetyl phosphate	143-149	C-X-C motif chemokine ligand 8	Homo sapiens	167-171
31719784-4	2018	Its toxicity is due to the ability of the compound to inhibit acetyl cholinesterase at cholinergic junction of the nervous system.	acetyl phosphate	62-68	butyrylcholinesterase	Homo sapiens	69-83
31897196-1	2020	Fibrinogen C domain-containing 1 (FIBCD1) is an acetyl-recognition receptor that affects the occurrence and development of certain tumors.	acetyl phosphate	48-54	fibrinogen C domain containing 1	Homo sapiens	0-32
31897196-1	2020	Fibrinogen C domain-containing 1 (FIBCD1) is an acetyl-recognition receptor that affects the occurrence and development of certain tumors.	acetyl phosphate	48-54	fibrinogen C domain containing 1	Homo sapiens	34-40
31905726-2	2019	It is a stoichiometric member of the minimal NuA4 histone acetyl transferase (HAT) complex consisting of EAF6, EPC1, ING3, and TIP60.	acetyl phosphate	58-64	enhancer of polycomb homolog 1	Mus musculus	111-115
31905726-2	2019	It is a stoichiometric member of the minimal NuA4 histone acetyl transferase (HAT) complex consisting of EAF6, EPC1, ING3, and TIP60.	acetyl phosphate	58-64	inhibitor of growth family, member 3	Mus musculus	117-121
31905726-2	2019	It is a stoichiometric member of the minimal NuA4 histone acetyl transferase (HAT) complex consisting of EAF6, EPC1, ING3, and TIP60.	acetyl phosphate	58-64	K(lysine) acetyltransferase 5	Mus musculus	127-132
31875566-7	2019	Here, we find that BRD4, an acetyl-histone-binding chromatin reader, inhibits the PCNA-unloading activity of ATAD5-RLC.	acetyl phosphate	28-34	bromodomain containing 4	Homo sapiens	19-23
31875566-7	2019	Here, we find that BRD4, an acetyl-histone-binding chromatin reader, inhibits the PCNA-unloading activity of ATAD5-RLC.	acetyl phosphate	28-34	proliferating cell nuclear antigen	Homo sapiens	82-86
31875566-7	2019	Here, we find that BRD4, an acetyl-histone-binding chromatin reader, inhibits the PCNA-unloading activity of ATAD5-RLC.	acetyl phosphate	28-34	ATPase family AAA domain containing 5	Homo sapiens	109-114
31875566-9	2019	BRD4-ATAD5 binds to acetyl-histones in nascent chromatin.	acetyl phosphate	20-26	bromodomain containing 4	Homo sapiens	0-4
31875566-9	2019	BRD4-ATAD5 binds to acetyl-histones in nascent chromatin.	acetyl phosphate	20-26	ATPase family AAA domain containing 5	Homo sapiens	5-10
31875566-11	2019	Disruption of the interaction between BRD4 and acetyl-histones or between BRD4 and ATAD5 reduces the PCNA amount on chromatin.	acetyl phosphate	47-53	bromodomain containing 4	Homo sapiens	38-42
31875566-11	2019	Disruption of the interaction between BRD4 and acetyl-histones or between BRD4 and ATAD5 reduces the PCNA amount on chromatin.	acetyl phosphate	47-53	proliferating cell nuclear antigen	Homo sapiens	101-105
31875566-13	2019	Thus, acetyl-histone-bound BRD4 fine-tunes PCNA unloading from nascent DNA.	acetyl phosphate	6-12	bromodomain containing 4	Homo sapiens	27-31
31875566-13	2019	Thus, acetyl-histone-bound BRD4 fine-tunes PCNA unloading from nascent DNA.	acetyl phosphate	6-12	proliferating cell nuclear antigen	Homo sapiens	43-47
31873180-0	2019	Sarcodia suieae acetyl-xylogalactan regulate RAW 264.7 macrophage NF-kappa B activation and IL-1 beta cytokine production in macrophage polarization.	acetyl phosphate	16-35	nuclear factor kappa B subunit 1	Homo sapiens	66-76
31873180-6	2019	Next, interleukin (IL) 1beta, TNF, and Malt-1 expression in RAW 264.7 macrophages treated with the S. suieae acetyl-xylogalactan was investigated through real-time quantitative polymerase chain reaction, and the results demonstrated that S. suieae acetyl-xylogalactan induced IL-1beta and Malt-1 expression.	acetyl phosphate	109-128	MALT1 paracaspase	Homo sapiens	39-45
31873180-6	2019	Next, interleukin (IL) 1beta, TNF, and Malt-1 expression in RAW 264.7 macrophages treated with the S. suieae acetyl-xylogalactan was investigated through real-time quantitative polymerase chain reaction, and the results demonstrated that S. suieae acetyl-xylogalactan induced IL-1beta and Malt-1 expression.	acetyl phosphate	109-128	interleukin 1 beta	Homo sapiens	276-284
31873180-6	2019	Next, interleukin (IL) 1beta, TNF, and Malt-1 expression in RAW 264.7 macrophages treated with the S. suieae acetyl-xylogalactan was investigated through real-time quantitative polymerase chain reaction, and the results demonstrated that S. suieae acetyl-xylogalactan induced IL-1beta and Malt-1 expression.	acetyl phosphate	109-128	MALT1 paracaspase	Homo sapiens	289-295
31861435-6	2019	Knockdown of maspin also enhanced tumorigenesis in vivo and downregulated protein levels of acetyl-histone H3.	acetyl phosphate	92-98	serpin family B member 5	Homo sapiens	13-19
31697807-0	2019	AMP-activated protein kinase links acetyl-CoA homeostasis to BRD4 recruitment in acute myeloid leukemia.	acetyl phosphate	35-41	protein kinase AMP-activated catalytic subunit alpha 2	Homo sapiens	0-28
31697807-0	2019	AMP-activated protein kinase links acetyl-CoA homeostasis to BRD4 recruitment in acute myeloid leukemia.	acetyl phosphate	35-41	bromodomain containing 4	Homo sapiens	61-65
31697807-3	2019	Here, we demonstrate that AMPK maintains the epigenome of MLL-rearranged AML by linking acetyl-CoA homeostasis to BET protein recruitment to chromatin.	acetyl phosphate	88-94	protein kinase AMP-activated catalytic subunit alpha 2	Homo sapiens	26-30
31697807-3	2019	Here, we demonstrate that AMPK maintains the epigenome of MLL-rearranged AML by linking acetyl-CoA homeostasis to BET protein recruitment to chromatin.	acetyl phosphate	88-94	lysine methyltransferase 2A	Homo sapiens	58-61
31547059-7	2019	Our results suggest that CPT1A supports CRPC by supplying acetyl groups for histone acetylation, promoting growth and antiandrogen resistance.	acetyl phosphate	58-64	carnitine palmitoyltransferase 1A	Homo sapiens	25-30
31857843-1	2019	YEATS-domain-containing MLLT1 is an acetyl/acyl-lysine reader domain, which is structurally distinct from well-studied bromodomains and has been strongly associated in development of cancer.	acetyl phosphate	36-42	MLLT1 super elongation complex subunit	Homo sapiens	24-29
31857843-2	2019	Here, we characterized piperazine-urea derivatives as an acetyl/acyl-lysine mimetic moiety for MLLT1.	acetyl phosphate	57-63	MLLT1 super elongation complex subunit	Homo sapiens	95-100
31730501-3	2019	In mice, Rev1 deleted in wbkC (Brucella lipopolysaccharide formyl-transferase) and carrying wbdR (E. coli acetyl-transferase) triggered antibodies that could be differentiated from those evoked by wild-type strains, was comparatively attenuated and protected against B. ovis, suggesting its potential as a B. ovis vaccine.	acetyl phosphate	106-112	REV1, DNA directed polymerase	Mus musculus	9-13
26264774-7	2015	As glucose-regulated lysine acetylation was predominant in central metabolic pathways and overlapped with acetyl phosphate-regulated acetylation sites, we deleted the major carbon regulator CRP and observed a dramatic loss of acetylation that could be restored by deleting the enzyme that degrades acetyl phosphate.	acetyl phosphate	106-122	catabolite gene activator protein	Escherichia coli	190-193
29105190-5	2018	Both functions require the lysine"s positive charge; intriguingly, the positive charge of K100 can be neutralized by acetylation using the central metabolite acetyl phosphate as the acetyl donor.	acetyl phosphate	158-174	complement C1q like 3	Homo sapiens	90-94
27848233-7	2016	The conducted studies also revealed that S. cerevisiae contains endogenous enzymes capable of breaking down acetyl-phosphate, likely into acetate, and that removal of the phosphatases Gpp1 and Gpp2 could largely prevent this breakdown.	acetyl phosphate	108-124	glycerol-1-phosphatase HOR2	Saccharomyces cerevisiae S288C	193-197
26681317-3	2015	Previous investigations have attempted to identify the phosphate donor of Rrp2, including the cognate histidine kinase, Hk2 (BB0764), non-cognate histidine kinases such as Hk1, CheA1, and CheA2, and small molecular weight P-donors such as carbamoyl-phosphate and acetyl-phosphate (AcP).	acetyl phosphate	263-279	rhomboid like 2	Homo sapiens	74-78
27738720-2	2017	In this study, an acetate kinase (ACK)/acetyl phosphate system was used to supply ATP and combined with Escherichia coli-overexpressed CMP kinase (CMK), NDP kinase (NDK), choline phosphate cytidylyltransferase (CCT), and choline kinase (CKI) to produce CDP-choline from CMP and choline chloride.	acetyl phosphate	39-55	cut like homeobox 1	Homo sapiens	253-256
26264774-7	2015	As glucose-regulated lysine acetylation was predominant in central metabolic pathways and overlapped with acetyl phosphate-regulated acetylation sites, we deleted the major carbon regulator CRP and observed a dramatic loss of acetylation that could be restored by deleting the enzyme that degrades acetyl phosphate.	acetyl phosphate	298-314	catabolite gene activator protein	Escherichia coli	190-193